Clinical case of the month. A rare case of Budd Chiari syndrome

Autor: Theepa, Thayalakulasingam, Rehan, Mohammed, Shibu, Varughese, Arthur, Zieske, David L, Smith, Lee S, Engel, Brian, Boulmay, Fred A, Lopez
Rok vydání: 2012
Předmět:
Zdroj: The Journal of the Louisiana State Medical Society : official organ of the Louisiana State Medical Society. 163(5)
ISSN: 0024-6921
Popis: Budd Chiari syndrome is a rare disorder resulting from hepatic venous outflow tract obstruction anywhere from the small hepatic veins to the suprahepatic inferior vena cava. This patient has a hypercoagulable state secondary to heterozygous mutation of factor V and the JAK2 mutation and is being anticoagulated. We hypothesize that the low protein C and low antithrombin III levels seen in this patient resulted from decreased synthetic function of the liver and were not indicative of actual deficiencies. Indeed, reports of coexisting protein C and antithrombin III deficiencies are not existent in the literature and likely are not compatible with life. All patients with BCS warrant a hypercoagulable work up and JAK2 mutation is increasingly recognized as a contributing factor, even in those patients without obvious signs of polycythemia vera.
Databáze: OpenAIRE